At 25°C, plots of the standard Gibbs energy change associated with the solvation of noble gases and aliphatic hydrocarbons vs. the size of the solutes prove to be approximately linear with a negative slope for common organic solvents but not for water. In the latter case, the plot has a characteristic V-shape. The slope is negative for noble gases, methane, and ethane, but is positive for larger alkanes. This means that the solubility of nonpolar solutes increases with solute size in every solvent except water. The solvation thermodynamics of noble gases and aliphatic hydrocarbons in five solvents (water, ethanol, benzene, c-hexane, and n-hexane) are analyzed in detail by a general theory, which is rederived to avoid risky misunderstandings. The calculations are performed in the same manner for all solvents, using simple formulas where the physical reliability is well established and the results are consistent. The work of cavity creation increases with solute size in every solvent, but to a far greater extent in water. Additionally, the work to turn on the solutesolvent attractive interactions increases in magnitude with solute size in every solvent, but to a lesser extent in water. By combining these two factors a satisfactory explanation for experimental data obtained emerges. The microscopic origins of the difference between water and common organic solvents are discussed.
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Giuseppe Graziano (2002) studied this question.
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